Project Manager – Laboratory

Job not on LinkedIn

🕒 July 16

🇦🇷 Argentina – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👷‍♀️ Project Manager

👻 Ghost score 33%

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Logo of ICON plc

ICON plc

10,000+ employees

Founded 1990

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.

📋 Description

• Coordinate project and programme management delivery • Resolve issues and develop team capability • Act as the Sponsor's main contact person regarding ICON services • Manage the day-to-day management of studies • Attend and represent ICON at Sponsor meetings • Manage 10–15 studies in accordance with Good Clinical Practice • Communicate study progress to Sponsors in a responsible and professional manner • Provide Sponsors with regular management reports • Provide ICOLAB support to sponsor personnel

🎯 Requirements

• Bachelor's degree in a relevant field such as life sciences or healthcare • Previous experience in project management within a laboratory or clinical research setting • Strong communication and interpersonal skills, with the ability to represent the company at sponsor meetings • Ability to manage multiple studies concurrently while ensuring adherence to regulatory standards and guidelines • Detail-oriented with strong organizational skills to effectively manage study documentation and timelines • Legal right to work in the country where the role is based

🏖️ Benefits

• Competitive base salary and performance related incentives • Health and wellbeing programmes including medical, dental, and vision coverage where applicable • Retirement and pension plans • Life assurance and disability coverage • Employee assistance programmes and wellbeing resources • Learning and development opportunities through structured training and career pathways

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